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Label-Free Composition Analysis of Supramolecular Polymer–Nanoparticle Hydrogels by Reversed-Phase Liquid Chromatography Coupled with a Charged Aerosol Detector

自愈水凝胶 化学 聚合物 纳米颗粒 聚己内酯 相(物质) 化学工程 色谱法 纳米技术 材料科学 高分子化学 有机化学 工程类
作者
Shijia Tang,Zachary Pederson,Emily L. Meany,Chun‐Wan Yen,Andrew K. Swansiger,James S. Prell,Bifan Chen,Abigail K. Grosskopf,Noah Eckman,Grace Jiang,Julie Baillet,Jackson D. Pellett,Eric A. Appel
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:96 (15): 5860-5868
标识
DOI:10.1021/acs.analchem.3c05747
摘要

Supramolecular hydrogels formed through polymer–nanoparticle interactions are promising biocompatible materials for translational medicines. This class of hydrogels exhibits shear-thinning behavior and rapid recovery of mechanical properties, providing desirable attributes for formulating sprayable and injectable therapeutics. Characterization of hydrogel composition and loading of encapsulated drugs is critical to achieving the desired rheological behavior as well as tunable in vitro and in vivo payload release kinetics. However, quantitation of hydrogel composition is challenging due to material complexity, heterogeneity, high molecular weight, and the lack of chromophores. Here, we present a label-free approach to simultaneously determine hydrogel polymeric components and encapsulated payloads by coupling a reversed phase liquid chromatographic method with a charged aerosol detector (RPLC-CAD). The hydrogel studied consists of modified hydroxypropylmethylcellulose, self-assembled PEG-b-PLA nanoparticles, and a therapeutic compound, bimatoprost. The three components were resolved and quantitated using the RPLC-CAD method with a C4 stationary phase. The method demonstrated robust performance, applicability to alternative cargos (i.e., proteins) and was suitable for composition analysis as well as for evaluating in vitro release of cargos from the hydrogel. Moreover, this method can be used to monitor polymer degradation and material stability, which can be further elucidated by coupling the RPLC method with (1) a multi-angle light scattering detector (RPLC-MALS) or (2) high resolution mass spectrometry (RPLC-MS) and a Fourier-transform based deconvolution algorithm. We envision that this analytical strategy could be generalized to characterize critical quality attributes of other classes of supramolecular hydrogels, establish structure–property relationships, and provide rational design guidance in hydrogel drug product development.
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